Control of Periodontal Infections
NCT01098448 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 187
Last updated 2010-04-02
Summary
The purpose of this study is to test combined effects of scaling and root planing with periodontal surgery, systemically administered amoxicillin and metronidazole, and/or local tetracycline on pocket depth reduction and attachment level "gain" in patients with chronic periodontitis.
Conditions
- Periodontitis
Interventions
- OTHER
-
scaling and root planing
scaling and root planing as a single therapy
- DRUG
-
local tetracycline
local delivery of tetracycline fibers releasing approximately 1.7 mg/tooth in all pockets \>5mm
- DRUG
-
systemic metronidazole and amoxicillin
systemic metronidazole (250 mg tid x 14) and amoxicillin (500 mg bid x 14
- OTHER
-
surgery
periodontal surgery in residual pockets of \>4mm
- DRUG
-
local antibiotics and systemic metronidazole and amoxicillin
1.7 mg/tooth tetracycline fiber plus metronidazole (250 mg tid x14d)and amoxicillin (500 mg bid x 14d)
- OTHER
-
local tetracycline and periodontal surgery
local delivery of tetracycline fibers releasing approximately 1.7 mg/tooth in all pockets \>5mm and periodontal surgery in residual pockets of \>4mm
- OTHER
-
periodontal surgery and systemic metronidazole and amoxicillin
surgery in residual pockets \>4mm and metronidazole (250mg tidx14d) and amoxicillin (500mg bidx14d)
- OTHER
-
surgery, local tetracycline, systemic metronidazole and amoxicillin
periodontal surgery in residual pockets \>4mm, tetracycline ibers releasing approximately 1.7 mg/tooth in pockets \>5mm, systemic metronidazlo (250mg tidx14d) and amoxicillin (500 mg bidx14d)
Sponsors & Collaborators
-
Göteborg University
collaborator OTHER -
Boston University
collaborator OTHER -
The Forsyth Institute
lead OTHER
Principal Investigators
-
J Max Goodson, DDS, PhD · The Forsyth Institute
-
Anne D Haffajee, BDS · The Forsyth Institute
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- FACTORIAL
Eligibility
- Min Age
- 20 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 1999-09-30
- Primary Completion
- 2004-12-31
- Completion
- 2004-12-31
Countries
- United States
Study Locations
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